Canonical Allele Identifier: CA2210135358

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150764T= , CM000678.2:g.16150764T=	GRCh38
NC_000016.9:g.16244621T= , CM000678.1:g.16244621T=	GRCh37
NC_000016.8:g.16152122T=	NCBI36
NG_007558.2:g.77708A=
NG_007558.3:g.77854A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*389A=	ENSP00000483331.2:n.*389A=
ENST00000205557.12:c.4217A= MANE Select	ENSP00000205557.7:p.Gln1406=
ENST00000640696.1:c.1031A=	ENSP00000492197.1:p.Gln344=
ENST00000205557.11:c.4217A=	ENSP00000205557.7:p.Gln1406=
ENST00000456970.6:c.3842A=	ENSP00000405002.2:n.3842A=
ENST00000576204.5:n.1080A=
ENST00000622290.4:c.*1426A=	ENSP00000483331.1:n.*1426A=
NM_001171.5:c.4217A=	NP_001162.4:p.Gln1406=
XM_011522479.1:c.4184A=	XP_011520781.1:p.Gln1395=
XM_011522480.1:c.3875A=	XP_011520782.1:p.Gln1292=
XM_011522481.1:c.3875A=	XP_011520783.1:p.Gln1292=
XR_933134.1:n.538+6474T=
NM_001351800.1:c.3875A=	NP_001338729.1:p.Gln1292=
NR_147784.1:n.3879A=
XM_011522479.2:c.4184A=	XP_011520781.1:p.Gln1395=
XM_011522481.3:c.3875A=	XP_011520783.1:p.Gln1292=
XM_017023212.1:c.4049A=	XP_016878701.1:p.Gln1350=
XM_024450261.1:c.4253A=	XP_024306029.1:p.Gln1418=
NM_001171.6:c.4217A= MANE Select	NP_001162.5:p.Gln1406=